Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.990 98 2002 2020
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.989 95 2002 2020
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.933 45 2002 2019
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 39 2002 2019
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 39 2002 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 24 2002 2018
dbSNP: rs121912664
rs121912664
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.941 17 2005 2018
dbSNP: rs1463038513
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.824 17 1998 2016
dbSNP: rs28934576
rs28934576
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 13 1993 2019
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 13 2006 2018
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.909 11 2005 2013
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.909 11 2002 2015
dbSNP: rs1799793
rs1799793
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.909 11 2002 2017
dbSNP: rs2292832
rs2292832
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.545 11 2011 2019
dbSNP: rs121913529
rs121913529
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 10 2009 2019
dbSNP: rs25489
rs25489
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.800 10 2004 2019
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 1.000 9 2012 2018
dbSNP: rs17879961
rs17879961
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 1.000 9 2006 2013
dbSNP: rs397517132
rs397517132
0.623 0.280 7 55191846 missense variant A/T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 1.000 9 2011 2019
dbSNP: rs9904341
rs9904341
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.080 1.000 8 2012 2020
dbSNP: rs231775
rs231775
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.070 0.857 7 2008 2018
dbSNP: rs61754966
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.070 0.857 7 2007 2013
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.070 1.000 7 2004 2016
dbSNP: rs1130409
rs1130409
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 0.833 6 2005 2015
dbSNP: rs121913500
rs121913500
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 1.000 6 2012 2018